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A resampling-based approach to share reference panels.
Cavinato, Théo; Rubinacci, Simone; Malaspinas, Anna-Sapfo; Delaneau, Olivier.
Afiliación
  • Cavinato T; Department of Computational Biology, University of Lausanne, Lausanne, Switzerland.
  • Rubinacci S; Swiss Institute of Bioinformatics, University of Lausanne, Lausanne, Switzerland.
  • Malaspinas AS; Division of Genetics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
  • Delaneau O; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Nat Comput Sci ; 4(5): 360-366, 2024 May.
Article en En | MEDLINE | ID: mdl-38745108
ABSTRACT
For many genome-wide association studies, imputing genotypes from a haplotype reference panel is a necessary step. Over the past 15 years, reference panels have become larger and more diverse, leading to improvements in imputation accuracy. However, the latest generation of reference panels is subject to restrictions on data sharing due to concerns about privacy, limiting their usefulness for genotype imputation. In this context, here we propose RESHAPE, a method that employs a recombination Poisson process on a reference panel to simulate the genomes of hypothetical descendants after multiple generations. This data transformation helps to protect against re-identification threats and preserves data attributes, such as linkage disequilibrium patterns and, to some degree, identity-by-descent sharing, allowing for genotype imputation. Our experiments on gold-standard datasets show that simulated descendants up to eight generations can serve as reference panels without substantially reducing genotype imputation accuracy.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Estudio de Asociación del Genoma Completo / Genotipo Límite: Humans Idioma: En Revista: Nat Comput Sci Año: 2024 Tipo del documento: Article País de afiliación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Estudio de Asociación del Genoma Completo / Genotipo Límite: Humans Idioma: En Revista: Nat Comput Sci Año: 2024 Tipo del documento: Article País de afiliación: Suiza